Donovan Kelsey M, Mahan Marielle, Murdock Narmien, Kolsky Martin P, Osborne Benjamin
Department of Ophthalmology, Georgetown University School of Medicine, Washington, DC, USA.
Department of Ophthalmology, MedStar Georgetown University Hospital, Washington, DC, USA.
Neurohospitalist. 2025 Aug 9:19418744251367172. doi: 10.1177/19418744251367172.
Myelin oligodendrocyte glycoprotein (MOG) antibody-associated optic neuritis is a demyelinating disease that shares clinical overlap with Neuromyelitis Optica Spectrum Disorder (NMOSD) and Multiple Sclerosis (MS). The immunosuppressive effects of pregnancy followed by a rebound in the immune system postpartum are thought to affect presentation and relapse rates of NMOSD and MS. Few studies exist describing pregnancy affecting MOG antibody-associated disease. In this case, a 29-year-old female from Ethiopia presented on postpartum day 8 with 4 weeks of progressive, painful bilateral vision loss that had acutely worsened over the past 6 days. Her visual acuity was light perception in the right eye and hand motion in the left eye with a right afferent pupillary defect. Dilated exam revealed bilateral optic nerve head elevation, vascular tortuosity, and macular folds. MRI of the brain and orbits with contrast revealed long segment bilateral optic nerve enhancement and nonspecific white matter changes. Serum MOG IgG was positive (1:160). Her vision rapidly improved with intravenous methylprednisolone 1000 mg daily for 5 days, followed by an oral prednisone taper. After 6 months, the patient's vision returned to 20/20 in each eye, and she has had no further clinical relapse. This case suggests that initial presentation of MOG optic neuritis may be affected by pregnancy. Physicians must appropriately triage patients with postpartum vision changes to ensure prompt treatment.
髓鞘少突胶质细胞糖蛋白(MOG)抗体相关视神经炎是一种脱髓鞘疾病,与视神经脊髓炎谱系障碍(NMOSD)和多发性硬化症(MS)存在临床重叠。孕期的免疫抑制作用以及产后免疫系统的反弹被认为会影响NMOSD和MS的临床表现及复发率。关于孕期影响MOG抗体相关疾病的研究较少。在此病例中,一名来自埃塞俄比亚的29岁女性在产后第8天就诊,有4周进行性、疼痛性双侧视力丧失,在过去6天内急剧恶化。她的右眼视力为光感,左眼视力为手动,右侧存在传入性瞳孔障碍。散瞳检查显示双侧视神经乳头隆起、血管迂曲和黄斑皱褶。脑部和眼眶增强MRI显示双侧视神经长节段强化及非特异性白质改变。血清MOG IgG阳性(1:160)。给予每日1000 mg静脉注射甲泼尼龙,持续5天,随后逐渐减量口服泼尼松,她的视力迅速改善。6个月后,患者双眼视力恢复至20/20,且未出现进一步的临床复发。该病例表明,MOG视神经炎的初始表现可能受孕期影响。医生必须对产后视力改变的患者进行适当分诊,以确保及时治疗。